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Pharmaceutical Books

Pioneers in the industry, we offer indian pharmacopoeia 2022, 9th edition, 4 vols. set, japanese pharmacopoeia, 18th edition - english version, ( 2 vols set ), european pharmacopoeia (ph. eur.) 11th edition, ( 3 volumes set ), 2023, rules and guidance for pharmaceutical manufacturers and distributors 2022 ( the mhra orange guide), u.s.pharmacopoeia: usp- nf - usb flash drive version and british pharmacopeia 2023 from India.

Indian Pharmacopoeia 2022, 9th Edition, 4 Vols. Set

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Indian Pharmacopoeia 2022, 9th Edition, 4 Vols. Set
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Approx. Rs 52,500 / SetGet Latest Price

Product Details:
Minimum Order Quantity1 Set
Name Of BookIndian Pharmacopoeia 2022, 9th Edition, 4 Vols. Set
Published ByIPC
Book NameIndian Pharmacopoeia 2022,9th Edition,4 Vols. Set
AuthorGovt. of India ( IPC )
LanguageEnglish
Edition9th Edition 2022
ISBN1
ColorOrange
StandardIndian
Year2022
Binding TypeHard Cover - 4 Vols. Set
Packaging Type4 Volumes Set
Product Code1
CoverHard Cover
BrandPharmaceutical Book
MaterialPharmaceutical Book
Country of OriginMade in India

The Indian Pharmacopoeia (IP) is published by the Indian Pharmacopoeia Commission (IPC) on behalf of Ministry of Health & Family Welfare, Government of India to fulfil the requirements of the Drugs and Cosmetics Act 1940. IP prescribes the official standards for drugs produced and/or marketed in India and thus contributes in the control and assurance of the quality of the medicines. The standards of the IP are authoritative and legally enforceable. It intends to help in the licensing of manufacturing, inspection and distribution of medicines in our country.

IP 2022 contains a total of 92 new monographs including 60 Chemical, 21 Vitamins, Minerals, Amino acids, Fatty acids etc., 3 Biotechnology-derived Therapeutic Products, 4 Human Vaccines, 2 Blood and Blood Related Products, 2 Herbs and Herbal Related Products, and 7 Phytopharmaceutical Ingredient Category monographs. This has led to the total number of 3152 monographs in the current edition of IP. In additions, 12 new general chapters have also been introduced.


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  • Packaging Details: Set of 4 Books
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Japanese Pharmacopoeia, 18th Edition - English Version, ( 2 Vols Set )

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Japanese Pharmacopoeia, 18th Edition - English Version, ( 2 Vols Set )
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Approx. Rs 63,000 / SetGet Latest Price

Product Details:
Minimum Order Quantity1 Set
Name Of BookU.S.Pharmacopoeia : USP - NF - USB Flash Drive Version
AuthorUSP
LanguageEnglish
Edition( USP-NF - USB Flash Drive Version )
Usage/ApplicationPharma Industry
Published ByUSP
Packaging TypeUSB Flash Drive Version
Book NameU.S. Pharmacopoeia: USP-NF - USB Flash Drive Version: USP 41-NF 36 and Subsequent Editions
Year2020
MaterialUSB Flash Drive Version

The English translation of the Japanese Pharmacopoeia (JP) 18th edition :

The Japanese Pharmacopoeia is the pharmaceutical standard that the Japanese Minister of Health, Labour and Welfare (MHLW) establishes to regulate the properties and quality of drugs.

As with other pharmacopoeias, the document is revised periodically. The 18th edition (JP18) came into effect on June 7, 2021. The text is originally prepared in Japanese and translated to English after the publication of the Japanese version. This usually is done within one year. According to the publication schedule, Supplement I to JP18 is to be published in December 2022 and Supplement II in 2024. It is planned that the 19th edition will be published in 2026.

Content of JP18 English Version

General Notice - General Tests, Processes and Apparatus
Official Monographs (A to L)
Official Monographs (M to Z)
Crude Drugs and Related Drugs
Infrared Reference Spectra
Ultraviolet-visible Reference Spectra
General Information


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European Pharmacopoeia (Ph. Eur.) 11th Edition, ( 3 Volumes Set ), 2023

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European Pharmacopoeia (Ph. Eur.) 11th Edition, ( 3 Volumes Set ), 2023
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Approx. Rs 49,500 / SetGet Latest Price

Product Details:
Minimum Order Quantity1 Set
Name Of BookEP : European Pharmacopoeia (Ph. Eur.) 11th Edition, 2023
AuthorEPC
LanguageEnglish
Edition11th Edition
Published ByEPC
BrandPharmaceutical Book - Main Volumes 11.0, Supplement 11.1, and Supplement 11.2
Book NameEuropean Pharmacopoeia (Ph. Eur.) 11th Edition, 2023
ColorBlue
StandardEPC
Year2023
Packaging Type3 Volumes Set - Main Volumes 11.0, Supplement 11.1, and Supplement 11.2
MaterialPharmaceutical Book

European Pharmacopoeia (Ph. Eur.) 11th Edition, 2023

Available to order from July 2022 / Effective from 1 January 2023

 The primary source for quality control standards

The European Pharmacopoeia (Ph. Eur.) is the primary source of official quality standards for medicines and their ingredients in Europe. Ph. Eur. standards provide a scientic basis for the quality control of a product throughout its life cycle, supporting the pharmaceutical industry and healthcare systems.

As laid down in the Council of Europe Convention on the Elaboration of a European Pharmacopoeia and in European Union and national pharmaceutical legislation, these standards are legally binding. They become mandatory on the same date in all states parties to the convention.

The 11th Edition key facts and figures

 

  •  New edition, legally binding in 39 European countries as of 1 January 2023 and applied in more than 130 countries worldwide.
  • Continually updated and modernised to meet users'''' needs. 
  • The 11th Edition of the Ph. Eur. contains:
    • 2 469 monographs (including dosage forms);
    • 386 general texts (including general monographs and methods of analysis);
    • and more than 2 800 descriptions of reagents.
  • Released in July 2022 and will be updated with eight periodic supplements over the following three years (11.1 to 11.8).

Print version
  • three initial volumes (11.0), followed by eight non-cumulative supplements (11.1 to 11.8);
  • available in either English or French;
  • now with QR codes for easier linking to the Knowledge database for each monograph and general chapter;
  • contains a subscription key (EPID code) giving access to the Ph. Eur. online archives.

Note that the 11th Edition print version will no longer contain change marks in revised and corrected texts.



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Rules And Guidance For Pharmaceutical Manufacturers And Distributors 2022 ( The MHRA Orange Guide)

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Rules And Guidance For Pharmaceutical Manufacturers And Distributors 2022  ( The MHRA Orange Guide)
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Approx. Rs 8,000 / BookGet Latest Price

Product Details:
Minimum Order Quantity1 Book
Book NameRules and Guidance for Pharmaceutical Manufacturers and Distributors 2022 (The MHRA Orange Guide)
AuthorMHRA: Medicines & Healthcare Products Regulatory Agency
LanguageEnglish
Edition2022
ISBN9780857114396
Number Of Pages1140 Pages
Binding TypePaperback
Size244x172mm
CoverSoft Cover
BrandPharmaceutical Book ( Pub: Pharmaceutical Press )

The 2022 edition of Rules and Guidance for Pharmaceutical Manufacturers and Distributors, known as "The MHRA Orange Guide”, is the essential reference for all manufacturers and distributors of medicines in the UK.
It provides you with a single authoritative source of European and UK guidance, information and UK legislation relating to the manufacture and distribution of human medicines, active substances, and brokering medicines.
The new 11th edition has been updated to incorporate changes made after the UK’s exit from the European Union on the 31st January 2020.
Comprehensive new content includes:
  • Amended extracts from the Human Medicines Regulations 2012 relating to:
  • manufacture, importation and assembly
  • wholesale dealing
  • brokering medicine
  • manufacturing, importing and distributing active substances

  • The Code of Practice for Qualified Persons, Guidance on Manufacture and Importation
  • UK guidance on complying with the EU guidelines on Good Distribution Practice for wholesale distributors and brokers of medicines and manufacturers, importers and distributors or active substances
  • UK guidance on: risk-based inspections, conditions of holding a manufacturer’s licence, wholesale dealer’s licence, a broker registration and an active substance registration, and controls on certain medicinal products.

New guidance on:
  • conditions of holding a manufacturing authorisation for investigational medicinal products,
  • importing guidance for investigational medicinal products from countries on a list to Great Britain,
  • Pharmaceutical Quality System expectations and Authorisation requirements for investigational medicinal products importation oversight,
  • list of approved countries for import,
  • pharmacovigilance for wholesalers,
  • the naming of sites on a wholesale dealer’s licence,
  • self-inspection for wholesale dealers and the responsible person for import.

Plus, revised GMP Annexes 2 and 17, and Commission guidance on principles and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections, for medicinal products for human use and for active substances for medicinal products for human use.
The MHRA Orange Guide is compiled by the Medicines and Healthcare products Regulatory Agency.


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U.S.Pharmacopoeia: USP- NF - USB Flash Drive Version

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U.S.Pharmacopoeia: USP- NF - USB Flash Drive Version
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Approx. Rs 1 Lakh / PackGet Latest Price

Product Details:
Minimum Order Quantity1 Pack
Name Of BookU.S.Pharmacopoeia : USP - NF - USB Flash Drive Version
AuthorUSP
LanguageEnglish
Usage/ApplicationPharma Industry
Edition( USP-NF - USB Flash Drive Version )
Published ByUSP
Packaging TypeUSB Flash Drive Version
Book NameU.S. Pharmacopoeia: USP-NF - USB Flash Drive Version: USP 41-NF 36 and Subsequent Editions
Year2020
MaterialUSB Flash Drive Version

U.S. Pharmacopoeia: USP–NF USB Flash Drive : Availavle


USP–NF USB Flash Drive :-

USP 41–NF 36 and Subsequent Editions

Technical Requirements

System Requirements:

  • One free USB 2.0 slot.
  • Close any screen capture program (e.g., SnagIT, Adobe Photoshop, Snipping Tool) currently open.

Operating Systems:

  • Windows only – XP and above

USP is aware of minor technical issues with the USP-NF English and Spanish USB drive format products. These issues are rare and most appear to be limited to systems running Windows 10. If you experience an "Access violation" error message while using the search function, please close the Lock Lizard application and restart. If you experience any other problems, please submit the webform.



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British Pharmacopeia 2023

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British Pharmacopeia 2023
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Approx. Rs 93,600 / SetGet Latest Price

Product Details:
Minimum Order Quantity1 Set
Name Of BookBritish Pharmacopeia 2023
AuthorMHRA
LanguageEnglish
Edition2023
Published ByTSO
BrandPharmaceutical Book
ColorMaroon
Year2023
Packaging TypeBox Packing ( 6 Hardback Volumes, Download, Online Access )

New, legally enforced standards, available from 1 August 2022. All European Pharmacopoeia texts included.

Updated annually, the British Pharmacopoeia (BP) is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products.

It includes approximately 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a BP monograph exists, medicinal products or active pharmaceutical ingredients sold or supplied in the UK must comply with the relevant monograph.

All monographs and requirements of the European Pharmacopoeia (Ph. Eur.) are reproduced in the BP, making the BP a convenient and fully comprehensive set of standards that can be used across Europe and beyond.

New for the BP 2023

The BP 2023 supersedes the BP 2022 and becomes legally effective on 1 January 2023. This edition incorporates new monographs from both the BP and Ph. Eur. along with a significant number of revised monographs.

Monographs and content:
  • 23 new BP monographs, 59 new Ph. Eur. monographs.
  • 151 amended BP monographs.
  • All monographs from the Ph. Eur. 10th edition as amended by Supplements 10.1 to 10.8 are included.
  • Ph. Eur. supplements 11.0, 11.1, and 11.2 included as in-year online and download product updates.

Ensure you get the best value access to the information you need. Choose from a range of flexible licences and formats - including full online and offline access.



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